lecture 66 Flashcards

Ott - pharmacotherapy of ADHD

1
Q

how does the etiology of ADHD mainfest?

A

multifactorial so environmental, genetics, and physiological all come into play
higher rate of diagnosis if a first-degree relative also has ADHD

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2
Q

what co-morbid conditions are associated with ADHD?

A

increased risk of SUD and antisocial personality disorder if ADHD is left untreated

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3
Q

when is it most likely that a person with ADHD will be diagnosed?

A

usually in childhood
but 1/3 of children will be diagnosed in adulthood

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4
Q

what is the diagnostic criteria for ADHD?

A
  1. for each symptom domain, must have at least 6 symptoms present and present in 2 or more settings
  2. for older adolescents and adults (17+), at least 5 symptoms are required for either of the two specifiers
  3. severeal inattentive or hyperactive symptoms must be present prior to age 12 years and present in 2 or more settings
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5
Q

how is inattention and hyperactivity/impuslivity defined in ADHD?

A

six or more of the following symptoms for at least 6 months inconsistent with developmental level and negatively impacting daily functioning

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6
Q

how are stimulants dosed in pediatric patients?

A

calculating based on mg/kg not found to be helpful as variations in dosing not found to be due to height or weight

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7
Q

for pts weighing under 16kg, what should the stimulants be dosed?

A

IR preferred due to limited low-dose availability of long-acting stimulants

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8
Q

when should stimulants be given?

A

avoid giving dose too late in the day (Due to insomnia)
may give an afterschool dose

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9
Q

what stimulant dosage form should be given for late afternoon symptoms?

A

longer-acting formulations

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10
Q

should two different stimulants be utilized?

A

no
can use two different dosage form of the same stimulant

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11
Q

when should 12.6 of Mydayis (mixed amphetamine salts) be used?

A

if pt age 13-17 with a CrCl between 15-30 mL/min

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12
Q

what is the formulation of daytrana (methylphenidate)?

A

patch

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13
Q

what is unique about vyvanse (lisdexfetamine)?

A

prodrug that is converted to dextroampetamine via first pass metabolism

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14
Q

what is unique about jornay (methylphenidate HCL)?

A

take dose in the evening between 6:30pm and 9:30pm

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15
Q

what are the AE of stimulants?

A

appetite loss
sleep disturbances
decreased growth
increase BP/HR

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16
Q

how would reduced appetite/weight loss be managed?

A

high-calorie meal when stimulant effects are low (breakfast, dinner)

17
Q

how would insomnia be managed?

A

dose earlier in the day
lower last dose of day or give earlier
consider sedating med at bedtime

18
Q

how should rebound symptoms be managed?

A

longer-acting stimulant trial
atomoxetine
antidepressants

19
Q

how should increased BP/HR be managed?

A

reduce dose
change stimulant

20
Q

how should hallucinations be managed?

A

d/c stimulant
reassess diagnosis

21
Q

how should risk for sudden cardiac death be managed?

A

risk no greater in clinical trials than general population
ass risk of cardiac structural abnormality and family hx
if concern, cardiac echo

22
Q

what should be monitored in stimulants?

A

appetite
behavior
BP
growth rate (height/weight)
HR
sleep ECG may be considered based on cardiac risk

23
Q

what drugs are alpha 2 agonists?

A

guanfacine ER
clonidine ER

24
Q

what is important to note about alpha 2 agonists?

A

must be tapered if d/c to avoid rebound HTN
guanfacine ER is a 3A4 substrate

25
Q

what drugs are NE reuptake inhibitors?

A

atomoxetine
viloxazine

26
Q

what is important to note about atomoxetine?

A

2D6 substrate
has weight based dosing for over an dunder 70 kg

27
Q

what is important to note about viloxazine?

A

capsules that need to be swallowed whole or put in applesauce
2D6/UGT substrate and strong 1A2 inhibitor

28
Q

what are the AE of NE reuptake inhibitors?

A

increase HR/BP
increase in suicidal thinking (BW)

29
Q

what are the SE of alpha 2 agonists?

A

decrease HR/BP, orthostasis
somnolence
dizziness
rebound HTN if abrupt D/c

30
Q

what drug classes make up non-stimulants?

A

alpha 2 agonists
NE reuptake inhibitors

31
Q

what are monitoring parameters for non-stimulants?

A

appetite
BP
HR
LFTs (atomoxetine only)

32
Q

what are important CP of bupropion?

A

not FDA-approved for ADHD
2D6 inhibitor
CI in seizure disorders and eating disorders

33
Q

what are important CP of TCAs?

A

less effective than methylphenidate
cardiac concerns - sudden cardiac death in children, lethal in overdose

34
Q

what is important to note about using mood stabilizer/atypical antipsychotics in ADHD therapy?

A

may be useful if there is comorbid BPD, conduct disorder, or intermittent explosive disorder
should not use as monotherapy to treat ADHD

35
Q

what is the first line treatment according to the AAP for preschool age children?

A

methylphenidate

36
Q

what is the treatment guidelines according to the AAP for elementary/middle school/adolescent?

A

first line – stimulants
second-line – atomoxetine, guanfacine ER, clonidine ER

37
Q

what is the AAP recommendation for adjunctive treatment?

A

only guanfacine ER and clonidine ER have evidence as adjunct to stimulants

38
Q

what is the NICE:ADHD guidelines 2018 for adults?

A

use Methylphenidate OR lidexamfetamine
then trial dextroamphetamine
then atomoxetine if no response